Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_assertion description "[Collectively, our study further elucidates the pathological effects of the G2019S mutation in the mammalian brain and supports the development of kinase inhibitors as a potential therapeutic approach for treating LRRK2-associated PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_assertion evidence source_evidence_literature NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_assertion SIO_000772 25731749 NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_assertion wasDerivedFrom befree-2016 NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_assertion wasGeneratedBy ECO_0000203 NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267513.RAcBg3AL0jKVpq7Wba2KMvjhsgEGnku92CuONdDsTDmvI130_provenance.